Medical Device Manufacturer · US , Fall River , MA

Teleflex Medical - FDA 510(k) Cleared Devices

40 submissions · 40 cleared · Since 2003

Recent clearances: Liquick X-treme, Liquick X-treme Plus, Hem-o-lok™ PurplePlus™ Large Polymer Ligating Clips, LMA Fastrach ETT SU

View 40 510(k) Devices ↓

40

Total

40

Cleared

0

Denied

FDA 510(k) Regulatory Record - Teleflex Medical Cardiovascular ✕

2 devices

1-2 of 2

Cleared Sep 18, 2024

Arrow® Nitinol Wire

Cardiovascular · 90d

Cleared May 05, 2006

INTRODUCER ASSEMBLY WITH ROTATOR LOCK

Cardiovascular · 67d